Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,612 recalls have been distributed to Nebraska in the last 12 months.
Showing 8281–8300 of 28,140 recalls
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology Recalled...
The Issue: Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cub 2 Enclosed Bed Canopy System Recalled by Sensory Medical Inc Due to Due...
The Issue: Due potential misuse of the product, firm is updating warnings and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VELYS Robotic-Assisted Solution Base Product No.: 451570100 Recalled by...
The Issue: System software v1.5.1 has a system software issue related to the Daylight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virus Counter Platform with Model Name VC3100 Recalled by Sartorius...
The Issue: The Virus Counter is an automated laboratory instrument that enables rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus 30 Priority Pack w/.096 RHV - WPL2122277-01 Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INDEFLATOR Plus 30 - WPL2122277-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 INDEFLATOR - WPL2122268-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 Priority Pack Accessory Kit/.096 RHV - WPL2122270-01 Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 Priority Pack w/COPILOT - WPL2122272-01 (2019-03-01) Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q Recalled by...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Microbiology Informatics Solution Recalled by Becton Dickinson &...
The Issue: When updating BD Kiestra customers to BD Synapsys version 4.10, the custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RocheDiabetes Care Platform Software version 2.5.2 material number...
The Issue: Potential for patient data mismatch when using browser "back" button to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.